Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs10494879
rs10494879
0.925 0.120 1 206778859 intron variant C/A;G snv 0.36
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2008 2008
dbSNP: rs11466782
rs11466782
0.925 0.120 5 157494947 intron variant A/G snv 0.10
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2011 2011
dbSNP: rs1800890
rs1800890
0.658 0.400 1 206776020 intron variant A/T snv 0.32
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2008 2008
dbSNP: rs1946518
rs1946518
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2017 2017
dbSNP: rs2071286
rs2071286
0.752 0.280 6 32212119 intron variant C/T snv 0.17
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2017 2017
dbSNP: rs2227307
rs2227307
0.851 0.240 4 73740952 intron variant T/G snv 0.45
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2014 2014
dbSNP: rs2395185
rs2395185
0.724 0.360 6 32465390 intron variant G/T snv 0.29
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2015 2015
dbSNP: rs2466571
rs2466571
0.925 0.120 1 207766701 intron variant G/T snv 0.46
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2014 2014
dbSNP: rs6676671
rs6676671
0.882 0.160 1 206779403 intron variant T/A snv 0.32
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2008 2008
dbSNP: rs708486
rs708486
0.925 0.120 14 52274253 intron variant A/G snv 0.35
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2011 2011
dbSNP: rs751837
rs751837
0.882 0.120 14 103018488 intron variant T/C snv 0.23
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2011 2011
dbSNP: rs9268853
rs9268853
0.790 0.440 6 32461866 intron variant T/C snv 0.29
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.800 1.000 1 2013 2013
dbSNP: rs948562
rs948562
11 58580292 intron variant A/G snv 0.15
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.800 1.000 1 2013 2013
dbSNP: rs2621416
rs2621416
0.882 0.280 6 32774091 intergenic variant T/C snv 0.26
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.800 1.000 1 2013 2013
dbSNP: rs273429
rs273429
8 131467654 intergenic variant C/T snv 0.43
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.700 1.000 1 2013 2013
dbSNP: rs4530903
rs4530903
6 32614112 intergenic variant C/T snv 0.10
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.800 1.000 1 2013 2013
dbSNP: rs707824
rs707824
0.925 0.120 6 14636732 intergenic variant T/C snv 0.74
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.810 1.000 1 2013 2013
dbSNP: rs9461776
rs9461776
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2017 2017
dbSNP: rs13181
rs13181
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2009 2009
dbSNP: rs267608150
rs267608150
0.851 0.320 7 5997388 stop gained AGGGGG/CTTCACAAC;CTTCACACACA;NNNNNNNNNNN delins
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.700 0
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.050 1.000 5 2004 2017
dbSNP: rs2230926
rs2230926
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.040 1.000 4 2013 2019
dbSNP: rs267601394
rs267601394
0.807 0.200 7 148811635 missense variant T/A;G snv
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.720 1.000 4 2012 2016
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.030 1.000 3 2012 2015